(R)-3-Amino-3-(4-isopropylphenyl)propanoic acid hydrochloride

95%

Reagent Code: #229232
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CAS Number 2703746-33-0

science Other reagents with same CAS 2703746-33-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.73 g/mol
Formula C₁₂H₁₈ClNO₂
badge Registry Numbers
MDL Number MFCD34186988
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of antiepileptic drugs, particularly in the production of (R)-phenibut derivatives. Its chiral structure makes it valuable in developing enantiomerically pure pharmaceuticals targeting the central nervous system. It is also employed in research for developing novel GABA analogs with improved blood-brain barrier penetration. Commonly utilized in medicinal chemistry for structure-activity relationship studies aimed at enhancing neuroactive agent efficacy.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,050.00
inventory 250mg
10-20 days ฿33,020.00

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(R)-3-Amino-3-(4-isopropylphenyl)propanoic acid hydrochloride
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Used as a key intermediate in the synthesis of antiepileptic drugs, particularly in the production of (R)-phenibut derivatives. Its chiral structure makes it valuable in developing enantiomerically pure pharmaceuticals targeting the central nervous system. It is also employed in research for developing novel GABA analogs with improved blood-brain barrier penetration. Commonly utilized in medicinal chemistry for structure-activity relationship studies aimed at enhancing neuroactive agent efficacy.

Used as a key intermediate in the synthesis of antiepileptic drugs, particularly in the production of (R)-phenibut derivatives. Its chiral structure makes it valuable in developing enantiomerically pure pharmaceuticals targeting the central nervous system. It is also employed in research for developing novel GABA analogs with improved blood-brain barrier penetration. Commonly utilized in medicinal chemistry for structure-activity relationship studies aimed at enhancing neuroactive agent efficacy.

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